59230-57-8 Usage
General Description
Cuminyl acetate is a chemical compound commonly found in essential oils and used in the flavor and fragrance industry. It is a colorless to pale yellow liquid with a sweet, herbal, and woody aroma. Cuminyl acetate is commonly used as a flavoring agent in food products, particularly in savory and spicy dishes, as well as in alcoholic beverages. It is also used in the production of perfumes, soaps, and cosmetics due to its pleasant and long-lasting fragrance. In addition, cuminyl acetate has been found to have antimicrobial properties and is being researched for potential applications in the pharmaceutical and medical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59230-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59230-57:
(7*5)+(6*9)+(5*2)+(4*3)+(3*0)+(2*5)+(1*7)=128
128 % 10 = 8
So 59230-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-9(2)12-6-4-11(5-7-12)8-14-10(3)13/h4-7,9H,8H2,1-3H3
59230-57-8Relevant articles and documents
Giordano,Belli
, p. 2314 (1979)
Rice husk ash: A new, cheap, efficient, and reusable reagent for the protection of alcohols, phenols, amines, and thiols
Shirini,Akbari-Dadamahaleh, Somayeh,Mohammad-Khah, Ali
, p. 577 - 586 (2014/06/09)
Amild, efficient, and eco-friendly protocol for the protection of alcohols and phenols as trimethylsilyl ethers has been developed using rice husk ash as a reagent. This reagent is also able to catalyze the acetylation of alcohols, phenols, thiols, and amines with acetic anhydride. All reactions were performed under mild conditions in good to high yields. Copyright
Acetylation of alcohols with acetic anhydride promoted by N,N,N-trimethylanilinium tribromide
Ghorbani-Choghamarani,Shiri,Rostami
, p. 1728 - 1730 (2014/08/05)
A wide variety of alcohols were reacted with acetic anhydride at room temperature in the presence of a catalytic amount of N,N,N-trimethylanilinium tribromide to produce the corresponding alkyl acetates in good to excellent yields. Following this procedure, acetylation of primary, secondary, and tertiary alcohols has been performed under neutral conditions.
